Compositions for prevention/prophylactic treatment of poison ivy dermatitis

ABSTRACT

The present invention, in one or more embodiments, comprises water-soluble derivatives of 3-n-pentadecylcatechol (poison ivy urushiol saturated congener) and/or 3-n-heptadecylcatechol (poison oak urushiol saturated congener) as compositions for the prevention and/or prophylactic treatment of contact dermatitis caused by poison ivy and poison oak. The present invention is also directed towards processes for making such compounds. Disclosed are compounds which are effective for tolerizing and desensitizing a subject against allergens contained in plants of the Anacardiaceae and Ginkgoaceae families comprising water soluble urushiol esters of general formula (I) Tolerizing and desensitizing mammals, including humans, to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families is attained by administering a composition containing at least one water soluble urushiol ester compound.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to compositions for the prevention and/or prophylactic and/or desensitization treatment of poison ivy dermatitis, methods of using such compositions, and methods of making such compositions.

2. Background of the Invention

Poison ivy (Toxicodendron radicans), poison oak (T. diversilobum), and poison sumac (T. vernix) affects 10-50 million Americans every year (1) and is the primary cause of occupational dermatitis in the United States (2). The prevalence of poison ivy and poison oak sensitivity in the general adult population ranges from 50% to 70% (3, 4). Peak frequency for sensitization occurs between ages 8-14 (5). Genetic susceptibility to urushiol sensitivity suggested that 80% of children who are born to two urushiol sensitive parents will become sensitive (6). Outdoor activities as well as outdoor occupations that relate to firefighting, forestry and agriculture are at high risk, costing significant medical expenses and worker's disability. Each fire season, approximately one third of forestry workers in California, Oregon and Washington are disabled by poison oak dermatitis (7). This disorder is very well known to most emergency and primary care physicians and dermatologists (8).

Other genera of the plant family Anacardiaceae with dermatogenic constituents include Anacardium (cashew nuts), Semecarpus (India ink tree), Metopium (poison wood), and Mangifera (mango). The allergenic components in most of these plants are 3-n-alk-(en)-yl catechols with C-15 or C-17 side chains and different degrees of unsaturation (0-3 olefinic bonds) (9-12). Urushiol is typical of such allergenic components present in poison ivy, poison oak, and the Asian lacquer tree (13). It has a catechol ring substituted with a C15 or C17 hydrocarbon chain at the 3 or 4 position, either saturated or having one, two or three unsaturated bonds (14). Both the catecholic ring and the aliphatic chain are proven to play important roles in allergenicity of urushiols (15-17). Contact of these catechols with the skin of susceptible individuals results in sensitization to all urushiols of the plant family Anacardiaceae (18). Once sensitivity is developed, it is difficult, if not impossible, to eliminate.

Allergic contact dermatitis (ACD) results from direct skin contact with a substance that the body recognizes as foreign. The resulting skin inflammation is a dendritic cell dependent delayed-hypersensitivity immunologic reaction. It occurs more commonly on thin-skin surfaces such as eyelids and genital skin. This type of response is elicited by cutaneous exposure to a variety of compounds that may act as haptens. These haptens become immunogenic after binding to discrete amino acid residues of proteins or peptides. The clinical manifestation is preceded by a sensitization phase, which is clinically silent. Rodent models of contact hypersensitivity have contributed towards understanding of mechanisms of ACD. It is known that during sensitization, dendritic cells (DCs) that have taken up an allergen/hapten (in this case urushiol) migrate to draining lymph nodes (LNs) where they mature, express co-stimulatory molecules, and present antigens to naive T cells (19-20). The mature DCs as well as the naive T cells are attracted to the LNs by chemokines that are expressed in the LNs (19, 21).

When a sensitized person is exposed to the hapten/urushiol, specific T cells (CD8+and CD4+) migrate under the influence of chemokines to the site of exposure on the skin where the cells undergo extensive proliferation (19). The activated T cells subsequently produce and release high levels of cytokines, thereby causing an inflammatory process leading to inflammation and/or edema. It has been suggested that CD8+cytotoxic lymphocytes are the main effector cells responsible for the manifestation of ACD. These cells are recruited early after challenge. CD4+T cell subsets are the down regulatory cells and are visible in the skin lesions after 72 hrs in the recovery phase of ACD (22). The percutaneous absorption of urushiol is similar to that of other lipophilic substances. These molecules preferentially enter the skin through the intercellular lipids of the stratum corneum. Any substance that blocks the contact of urushiol with the stratum corneum and prevents its entry, also known as barrier products, would likely offer some protection. Many commercial products have been developed and tested for their effectiveness in preventing urushiol dermatitis, and these experiments have been published (1, 23-28). Presently, only a few substances offer some realistic benefits (1, 23, 24).

One product (an organoclay, quanterium-18 bentonite) was tested by Epstein (23) in a pilot study and was found to be more effective than bentonite, kaolin or silicone in preventing experimental urushiol dermatitis. In 1992, Grevelink et al., (24) published the best contemporary review concerning the effectiveness of barrier products. They also compared the efficacy of seven commercial products in preventing experimental urushiol dermatitis in twenty volunteers using a 9-point global severity score. Stokogard (Stockhausen, Greenboro, N.C.), Hollister Moisture Barrier (Hollister, Inc., Libertyville, Ill.), and Hydropel (C&M Pharmacol, Inc., Hazel Park, Mich.) offered a substantial degree of protection. These products provided 59%, 53%, and 48% protection, respectively. Ivy Shield (Interpro, Inc., Haverhill, Mass.), Shield Skin (Mantor Corp., Minneapolis, Minn.), Dermofilm (Innovetec, Brussels, Belgium), and Uniderm (Smith and Nephew, Inc., Largo, Fla.) provided much lower (if any) levels of protection at 22%, 13%, 3%, and 9%, respectively (24). Topical Skin Protectant (TSP), another skin barrier product, is composed of polytetrafluoroethylene (PTFE) resins mixed in perfluorinated polyether oil (29). Vidmar and Iwane reported that TSP completely prevented dermatitis altogether in 34 of the 192 paired test sites and attenuated it to only trace levels in 22 paired sites (29).

Treatment for dermatitis is primarily symptomatic. For patients with severe cases, a tapering dose of oral corticosteroids such as prednisone may be used. Prednisone is a corticosteroid hormone (glucocorticoid) which decreases the immune system's response to various diseases to reduce symptoms such as swelling and allergic-type reactions. However, available “dosepacks” of corticosteroids are of little use since they deliver small doses of corticosteroid for too short a period of time and often result in a rebound reaction (30).

The remaining treatments for poison ivy related ACD are centered around palliative care. Benadryl® topical cream (Pfizer) dries the oozing and weeping of poison ivy, poison oak, and poison sumac and temporarily relieves the pain and itching.

There have been multiple desensitization regimens (elimination of sensitivity of sensitized individuals) utilized since the 1950s containing extracts of poison ivy/oak yet none are reliably effective (31, 32). The techniques consisted of ingestion or parenteral injection of various formulations of urushiol. Although some reports have described success (31, 32), the levels of desensitization were variable and not durable. In addition, the regimens produced mucous membrane, cutaneous, and systemic side effects. Accordingly, this approach has been largely abandoned.

Hyposensitization (reduction of the degree of sensitivity of sensitized individuals; tolerized) by administration of plant extracts is difficult to obtain. It requires large doses and months or years to be produced, and sensitivity is rapidly regained upon cessation of treatment (18, 31). The benefits and safety of the use of Rhus extracts (containing the active allergenic ingredient urushiols) for this purpose have been topics of dispute since they were first administered in 1917. Several reviews pertaining to the clinical use of Rhus extracts and allergens have been written (23, 33, 34).

The reason for the lack of activity of administered urushiols in the free form might be due to the high reactivity of the catechol moiety of the urushiols with plasma proteins. Putatively, once absorbed, the urushiols bind irreversibly with the proteins and become “deactivated”. We have rationalized that it might be necessary for the urushiols to bind to cell membranes to be effective in the production of tolerance or the prophylactic treatment of poison ivy dermatitis. Taking this into account, we previously prepared a conjugate of poison ivy urushiol bound to cell membranes by spiking the urushiol solution into a suspension of blood cell membranes from lyzed and washed blood cells and then reinjected the suspension into donor animals (18). We have shown (18) that tolerance was produced by the administration of 3-n-p entadecylcatechol (the saturated congener of poison ivy urushiol) coupled to red blood cell membranes in guinea pigs. The treated group was tolerant to 3-n-pentadecylcatechol for the 20 weeks of the study.

Having succeeded in that approach, we theorized that administration of a urushiol ester might be more effective in that some of the ester could hydrolyze at the surface of the blood cells, thereby resulting in free urushiol which could bind to the membrane. Administration of a urushiol ester can be through for example subcutaneous injection (“s.c.”), intramuscular injection (“IM”), intravenous injection (“IV”), intranasal administration, transmucosal administration and rectal administration. Tolerance to poison ivy urushiol in the guinea pig model was accomplished by IV injection of the diacetate esters of poison ivy and oak urushiols in naïve guinea pigs and complete desensitization or hyposensitization was accomplished in sensitized animals by the same treatment (35). The efficacy of oral administration of poison ivy and poison oak urushiols was compared with the use of the respective esterified derivatives for desensitizing sensitive guinea pigs (36). The esterified derivatives produced a greater degree of hyposensitization than was produced by the free urushiols and the hyposensitization was of longer duration. We have concluded that for the urushiol esters to be most effective, parental administration is necessary. We, therefore, conducted a study to evaluate the potential for a single-dose regimen to be effective for hyposensitization to poison ivy urushiol dermatitis (37). Hyposensitization was accomplished in a single intramuscular dose of 20 mg.

The use of oil as a vehicle for administration of esterified urushiol presents major limitations both in terms of the route of administration (limited to intramuscular) and efficiency of drug delivery by acting as a depot with slow release that might not be as effective as administering an IV or subcutaneous injection. Therefore, the development of effective water-soluble derivatives of urushiol (or its saturated congener) represents a viable improvement and an option for a successful product for the prevention of poison ivy/poison oak contact dermatitis.

The mechanism of action for the prophylactic treatment of poison ivy/oak dermatitis using urushiols is not known but may involve the up-regulation of CD4+T cell proliferation with concomitant downregulation of CD8+T cells.

SUMMARY OF INVENTION

The present invention, in one or more embodiments, comprises water-soluble derivatives of poison ivy urushiol or 3-n-pentadecylcatechol (poison ivy urushiol saturated congener) and/or poison oak urushiol or 3-n-heptadecylcatechol (poison oak urushiol saturated congener) as compositions for the prevention and/or prophylactic treatment of contact dermatitis caused by poison ivy and poison oak and other ACD causing plants of the family Anacardiaceae and Ginkoaceae. Further, the present invention is directed towards processes for making such compounds. In particular, there are disclosed compounds which are effective for tolerizing and desensitizing against contact dermatitis caused by allergens contained in plants of the Anacardiaceae and Ginkgoaceae families comprising water soluble urushiol esters of the general formula (I)

wherein R₁ is an alkyl radical having 11 to 19 carbon atoms, or an unsaturated congener thereof; or mixtures thereof; and R₂ and R₃ are each independently the residue radicals derived from an amino acid or combination of amino acids (i.e. di, tri, or poly peptide residue), a carbamate forming compound or a sulfate or phosphate ester or an ester of a dicarboxylic acid, resulting in a salt forming compound with water soluble characteristics. Suitable substituent groups include compounds in which R₁ is pentadecyl, heptadecyl, nonadecyl, mono-olefinic pentadecyl, mono-olefinic heptadecyl, diolefinic pentadecyl, diolefinic heptadecyl, triolefinic pentadecyl and triolefinic heptadecyl.

The present invention is also directed towards a method of tolerizing and desensitizing mammals, including humans, to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families which consists essentially of administering to said mammal a composition comprising a compound or mixture of compounds as disclosed in the present invention. In the context of this application, desensitization is meant to encompass elimination of sensitivity in a sensitized subject as well as a reduction in the degree of sensitivity of a sensitized subject (hyposensitization or tolerization). Also disclosed are methods of preparing the compositions of this invention.

DETAILED DESCRIPTION OF THE INVENTION

A strategy was developed comprising water-soluble ester derivatives of urushiol. Said derivatives are able to quickly reach the blood stream following administration and hydrolyze at the surface of the blood cells resulting in the generation of active, free urushiol, which can then bind to cell membranes. The urushiol-cell membrane conjugate is believed to be the active entity causing desensitization.

By amino acid esters is meant esters of urushiols and urushiol cogeners in which the phenolic groups are esterified with a compound having a carboxy group capable of forming such esters as well as an amino group which can be transformed into a pharmaceutically acceptable salt form in the amino acid ester final product.

By an urushiol “amino acid ester” is meant, for example urushiol mono- or di-alaninate. The amino group or groups may, of course, have originated from any amino acid, poly(amino acid) or peptide.

Useful compounds to make the present amino acid esters include both natural and synthetic amino acids as well as di-, tri- or polypeptides.

Useful amino acids include, for example, Alanine, Arginine, Asparagine, Aspartic Acid, Cysteine, Glutamine, Glutamic Acid, Glycine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Proline, Serine, Threonine, Tryptophan, Tyrosine, Valine, Homoserine, Homoserine lactone, and Norleucine.

By carbamate derivatives of urushiol is meant urushiol derivatives in which the phenolic hydroxy groups are converted to carbamate linkage and the residue of the carbamate forming material includes a carboxy group which can be transformed into a pharmaceutically acceptable salt.

By a “dicarboxylic acid” here is meant an organic acid that has two carboxyl groups (—COOH). Suitable dicarboxylic acids in this invention are, for example, malonic acid, malic acid, glutaric acid and its derivatives, and succinic acid. Dicarboxylic acid includes also anhydrides and reactive derivatives of dicarboxylic acids such as, for example, dicarboxylic acid halides.

Compounds are disclosed which are effective for desensitizing a subject against contact dermatitis caused by allergens contained in plants of the Anacardiaceae and Ginkgoaceae families comprising water-soluble urushiol esters of the following formula I

wherein R₁ is an alkyl radical having 11 to 19 carbon atoms, or an unsaturated congener thereof; or mixtures thereof; and R₂ and R₃ are each independently the residue radicals derived from an amino acid or a combination of amino acids, a carbamate-forming compound, an ester of a dicarboxylic acid or a dicarboxylic acid derivative or a sulfate or phosphate ester wherein the esters are salt forming compounds.

R₁ of forumla I can be pentadecyl, heptadecyl, or nonadecyl.

The compounds of formula I can be esters of amino acids or combinations of amino acids or derivatives of an amino acid with a dicarboxylic acid, esters formed via dicarboxylic acids or dicarboxylic acid derivatives, phosphate or sulfate esters, or carbamate esters which are salt-forming carbamates.

Illustrative but not limiting compounds include heptadecyl catechol phenyl alaninate ester, 3-hepta-1,2-phenylene bis (4-aminophenyl) butanoate, heptadecyl catechol indole-propionate ester, heptadecyl catechol-β-alaninate ester, pentadecyl catechol valininate ester, pentadecyl catechol-di-valininate ester, pentadecyl catechol glutaminate ester, pentadecyl catechol asparaginate ester, pentadecyl catechol glutaminate-β-alanine dipeptide ester.

The invention also encompasses pharmaceutical compositions containing at least one water soluble compound according to formula I and suitable pharmaceutical carrier therefor.

These pharmaceutical compositions are adapted to be administered parenterally, transdermally or intranasally.

The invention further encompasses a method of desensitizing a subject to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families which comprises administering to said subject a composition comprising a compound or mixture of compounds according to formula I.

The method of treatment can be by parenteral, transdermal or transnasal administration to a subject.

The present method of desensitizing a subject to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families comprises administering to said subject, of a pharmaceutical composition containing a water soluble compound or mixture of water soluble compounds according to formula I.

The invention further provides a method of preparing compounds according to the invention by reacting a compound of the formula II

wherein R₁ is as defined above, with a protected amino acid or a combination of protected amino acids or a derivative of a protected amino acid with a dicarboxylic acid or dicarboxylic acid derivative followed by removal of the protective group.

Furthermore, the invention encompasses method of preparing compounds according to the invention comprising reacting a compound of the formula II

wherein R₁ is as defined above, with a dicarboxylic acid or dicarboxylic acid derivative.

Additionally the invention encompasses a method of preparing compounds according to the invention comprising reacting a compound of the formula II

wherein R₁ is as defined above, with para nitrophenyl chloroformate followed reaction of this intermediate with an allyl ester of a amino acid or combination of amino acids followed by removal of the allyl group.

A further embodiment is a method of making the sulfate esters according to the invention comprising reacting a compound of the formula II

wherein R₁ is as defined above, with chlorosulfonic acid.

The following experimental describes methods of preparing the water-soluble derivatives of the present invention. A person of skill in the art will recognize that these preparatory methods are broadly applicable to the preparation of various ester derivatives of urushiol. Accordingly, the proceeding methods are exemplary. Further, a person of skill in the art will also recognize that methods of tolerization and/or densensitization are also broadly applicable.

Experimental

Water-soluble derivatives may be and were evaluated based on synthetic yields, water solubility, and purity as criteria for suitability. Further, derivatives may be and were tested for efficacy in producing tolerance to sensitization to poison ivy/poison oak urushiols in the guinea pig animal model. It is well-recognized in the art that successful treatment by use of a medicament or other agent in an animal model, such as the guinea pig animal model of the current invention, is strongly correlative to effects in other animal models including humans.

Synthesis of Water Soluble Derivatives of Urushiols

Four different types of water-soluble derivatives of urushiols can be prepared, namely amino acid esters, dicarboxylic acid esters, carbamates with free terminal carboxylic groups, and sulfate and phosphate esters. Other groups which satisfactorily provide water-solubility to the urushiols and appropriate bioactivity, including hydrolyzation ability in-vivo are also contemplated. Accordingly, the proceeding products are also exemplary. These products can be purified using different chromatographic techniques such as column chromatography, thin layer chromatography, and high performance liquid chromatography. Spectral analysis using, for example, Mass Spectrometry (MS), ¹H-NMR, Infrared/Ultraviolet Spectral Analysis (e.g. FTIR), and ¹³C-NMR along with melting point and elemental analysis, can carry out structural confirmation.

Synthesis of Amino Acid Esters of Urushiols

Pentadecyl catechol (PDC, 1) and heptadecyl catechol (HDC, 2) (the saturated congeners of poison ivy and poison oak urushiols, respectively) can be used to prepare esters with different amino acids such as, those depicted in structures 3-12. Other amino acids and amino acid radicals (di, tri or polypeptides) are also contemplated.

The starting materials (1 and 2) can be prepared by hydrogenation of purified poison ivy and poison oak urushiols, respectively. Alternatively, compounds 1 and 2 are prepared synthetically as exemplified in procedures 1, 2, and 3 as described in examples 1-3. Unsaturated congeners are also contemplated starting materials, e.g., unsaturated congeners of compound (1) or (2) may be derivatized to form unsaturated-catechol derivatives.

(1) or (2) can be dissolved in dichloromethane (DCM), and an amino acid (2.2 eq), such as one mentioned above, can be added to the solution. Catalytic amounts of dimethyl-aminopyridine (4-DMAP, e.g., 0.1 eq), along with dicyclohexylcarbodiimide (DCC, 2.2 eq) can then be added and the reaction mixture allowed to stir until thin-layer chromatography (TLC) confirms the complete conversion of the starting material to the product.

Suitable staining agents and other detection means, including ultraviolet analysis of the TLC plate, may be used and persons of skill in the art would readily be able to determine such agents and/or techniques. Exemplary techniques include: ferric chloride as a monitoring agent, wherein free catechols give an immediate, distinct dark blue color.

Pretreatment of the TLC plate is also within the skill of one of the art and includes use of 1N NaOH, as a plate-spray, to induce alkaline hydrolysis of esters, prior to staining with ferric chloride. Again, suitable workup techniques are within the skill of the art, and include reaction filtration, separation or washing as by use of a separatory funnel and suitable solvents, drying of organic solvents such as with magnesium sulfate or sodium sulfate, and concentration such as by rotary evaporation.

Products protected by N-tert-butoxycarbonyl (t-Boc) are, preferably, to be purified primarily by column chromatography on silica gel with monitoring of fractions by any suitable technique including TLC.

Deprotection of T-Boc

Anhydrous tetrahydrofuran (THF) is to be bubbled with HCl gas to saturation. Excess HCl gas is flushed with nitrogen. The t-Boc derivatives can then be dissolved in anhydrous THF. This is followed by the dropwise addition of acidic THF. After addition of all acidic THF, the mixture is to be allowed to stir at room temperature until complete deprotection is confirmed by TLC or any other suitable technique. The solvent is then evaporated. Acetone is then added to the residue and the mixture is to be stored in the freezer overnight. In the morning, the solid product thus obtained is filtered. This crystallization procedure may be repeated for complete recovery of the product (Scheme 1). Some amino acid esters of 1 and 2 may have high solubility in acetone and therefore may not crystallize. In these cases, the solvent is to be evaporated to produce the solid product which is to be crystallized from an appropriate solvent.

In addition to mono amino acid derivatives, this invention also covers derivatives with two, three or more amino acids (di, tri, or poly peptide derivatives). Such derivatives might have enhanced stability in addition to their water solubility. Synthesis of dipeptide derivatives follow the same procedure described for the mono derivatives where by the mono derivative is used to add another amino acid to make the dipeptide and the dipeptide used to add another amino acid to form the tripeptide derivative etc. This is depicted in the general scheme below. Alternatively for the polypeptide derivative, the polypeptide itself is first synthesized to the desired length followed by reacting the polypeptide directly with compound 1 or 2 to form the desired product.

Synthesis of Carbamates of Urushiols

Pentadecyl catechol (1) and heptadecyl catechol (2) can be used to make different carbamates using the following general procedure as outlined in Scheme 2.

The starting material is dissolved in freshly distilled DCM and DMAP and triethylamine added, followed by 4-nitrophenyl-chloroformate. The reaction can be monitored by TLC for completeness. When complete, 4-aminobutyric acid allyl ester or 6-aminohexanoic acid allyl ester or 4-(4-aminophenyl) butyric acid allyl ester dissolved in DCM are to be added dropwise to form the allyl esters of the final products 9-11 respectively. TLC can again monitor the reactions for completion. The protected products can be purified by different chromatographic techniques.

Deprotection of the Allyl Esters of the Carbamates

The products can be dissolved in DCM and phenylsilane added to the solution along with triphenylphosphine. The reaction mixture is to be allowed to stir at room temperature and can be monitored by TLC for completion. Methanol (MeOH) is then to be added and stirring continued for another 15 minutes. The solvent is then evaporated and the product purified using chromatographic techniques.

Synthesis of the Sulphate Esters of the Urushiols

The starting material (1 or 2) can be dissolved in anhydrous toluene, cooled to and maintained at −16 to −18° C. While maintaining the temperature chlorosulfonic acid is to be added dropwise over a period of 30 minutes. The reaction is then allowed to stir until completion as indicated, e.g., by TLC. Once the reaction is complete, 0.1N HCl is to be added and the mixture extracted with DCM three times. The organic layers will be combined and evaporated to dryness. The product (16, starting from 2) may be purified using different chromatographic techniques.

Sulfuric acid mono-(3-heptadecyl-2-sulfooxy-phenl)ester-16

EXAMPLES Example 1 Synthesis of penta or hepta decyl catechol (PDC or HDC) (Procedure 1)

To a solution of 2,3-dihydroxy benzaldehyde in anhydrous ethanol was added anhydrous K₂CO₃ along with catalytic amount of iodine and stirred at 5° C., while benzyl chloride was added drop wise.

The mixture was refluxed while stirring for 3 hours and then additional benzyl chloride was added and refluxed for another 2 hours.

The solvent was evaporated and the residue was partitioned between ether and water. The organic solution was washed with water and dried over sodium sulfate. All volatiles were evaporated on high vacuum and the product was obtained as light yellow solid material. The yield was quantitative.

The tetradecyl Grignard reagent was prepared in the usual way from tetradecyl bromide, magnesium and trace of iodine in ether. To this solution at reflux was added 2,3 dibenzyloxy-benzaldehyde in ether. After the addition the mixture was refluxed for 4 hours, cooled, treated at 22° C. with 12% hydrochloric acid. The layers were separated and the organic layer was washed twice with water and then with brine. The solvent was evaporated to produce an oily crude product which was dissolved in ice cold methanol and the precipitated waxes were filtered.

Hydrogenation of 2,3 dibenzyloxy-tetradecyl benzyl alcohol or 2,3 dibenzyloxy-hexadecyl benzyl alcohol was carried out with 10% Pd/C catalyst and conc. H₂SO₄ at 200 PSI and 125° C. to produce pentadecyl catechol (1) or heptadecyl catechol (2).

Example 2 Synthesis of penta or hepta decyl catechol (PDC Or HDC) (Procedure 2)

The tetradecyl Grignard reagent was prepared in the usual way from tetradecyl bromide (3.3 mmole), magnesium (3.5 mmole) and a trace of iodine in 3 L of ether. To this was added at reflux a solution of 2,3-dimethoxy-benzaldehyde (2.9 mmole) in 1L of ether. After the addition, the mixture was refluxed for 4 hours, cooled, treated at 20° C. with 3 L of 12% HCl, the layers separated, and the organic layer washed twice with water and then once with brine. The ether was then rotaevaporated leaving a syrup which was dissolved in 2L of MeOH. After cooling in an ice bath overnight the precipitated waxes were filtered. The crude product was isolated from the filtrate by rotaevaporation of all volatiles. The yield was quantitative.

2,3-Dimethoxy-1-tetradecylbenzyl alcohol (1.7 mmole, crude) in 1.5 L of ethyl acetate was hydrogenated with 10 g 10% Pd/C catalyst and 10 mL of conc. H₂SO₄ at 200 PSI and 125° C. The reaction was complete in 4-6 hrs. The catalyst was filtered. The filtrate was washed twice with water and once with brine. After drying over MgSO₄ the solvent was rotaevaporated and residual oil distilled. Considerable material (unidentified) was obtained up to 160° at 0.1 Torr. The product was then collected at 165-195° at 0.2 Torr.

2,3-Dimethoxy-6-pentadecyl-catechol (0.9 mmole) in 500 mL of glass-distilled methylene chloride (DCM) was added dropwise at −20 to −10° to a stirred solution of boron tribromide (BBr₃) (2.4 mmole) in 2L of glass distilled DCM in a nitrogen atmosphere. After the addition was complete, the mixture was stirred overnight at room temperature. Methanol was added at 10° to 20°. The mixture was warmed to 30° to 40° under a strong stream of nitrogen to remove much of the hydrogen bromide present. Crystallization was used to purify the product.

Example 3 Synthesis of penta or hepta decyl catechol (PDC or HDC) (Procedure 3)

An alternate to the Grignard's reaction described in the above procedures, Wittig reaction was used to form an olefin as shown below followed by appropriate steps to yield the desired product.

All the compounds formed were analyzed on HPLC for their purity (>99.5%).

Example 4 Preparation of HDC-phenyl alaninate ester (3)

Heptadecyl catechol (HDC, 2, 0.25 g) was dissolved in 20 mL of DCM, and t-boc-L-phenyl-alanine (2.2 eq) was added to the solution. A catalytic amount of DMAP, and DCC (2.2 eq) was then added and the reaction mixture was allowed to stir until TLC confirmed complete conversion of the starting material to the product.

Ferric chloride was used as reagent to monitor the reaction mixture on TLC, where the free catechols gave immediate distinct dark blue color with the reagent. However, the esters needed base hydrolysis before producing the color. 1 N NaOH was used as a second spray to hydrolyze the esters and locate the spots of the esters. Upon completion of the reaction, the reaction mixture was filtered to get rid of the majority of the reagents, and the solvent was then evaporated. The t-boc-protected product was purified using column chromatography on silica gel and the collected fractions were monitored by TLC.

Anhydrous THF was bubbled with HCl gas to saturation. Excess HCl gas was flushed with nitrogen. The t-boc derivative was dissolved in anhydrous THF, and acidic THF was added drop-wise. After addition of all the acidic THF, the mixture was allowed to stir at room temperature until completely deprotected as confirmed by TLC. The solvent was then evaporated and acetone was added to the residue. Upon storage of the mixture in the freezer overnight, a solid product, was obtained by filtration. This crystallization procedure was repeated to get 239 mgs of the product (73%).

The product was confirmed by HREIMS (TOF) m/z 643.4470 [M+H]⁺(calculated for C₄₁H₅₈N₂O₄, 643.4475) and other spectral techniques.

Water Solubility of HDC-Phenyl Alaninate Ester

HDC-phenyl alaninate (10 mg) formed a homogenous solution when dissolved in 50 ul of ethanol and the resulting solution adjusted to 1 ml with water.

Example 5 Preparation of 3-hepta-1,2-phenylene bis (4-aminophenyl) butanoate (4)

Heptadecyl catechol (HDC, 2, 0.15 g) was dissolved in 10 mL of DCM, and 4-amino-phenyl-butyric acid (2.2 eq.) was added to the solution. A catalytic amount of DMAP and DCC (2.2 eq.) was then added and the reaction mixture was allowed to stir until TLC confirmed complete conversion of the starting material to the product (also referred to as HDC-4-(4-aminophenyl)-butyrate ester), 4.

The reaction mixture was worked up as usual and the product was purified using column chromatography on silica gel. The fractions containing the product were combined to give 144 mgs of the product (89%).

The product was confirmed by HREIMS (TOF) m/z 671.4788 [M+H]⁺ (calculated for C₄₃H₆₃N₂O₄, 671.4970) and other spectral techniques.

10 mg of 3-hepta-1,2-phenylene bis (4-aminophenyl) butanoate was a clear solution when dissolved as a HC1 salt in 50 ul of ethanol and the resulting solution adjusted to 1 mL with water (10mg/mL).

Synthesis of urushiol esters having terminal carboxylic functions:

Example 6

Preparation of 5,5′-(3-heptadecyl-1,2-phenylene)bis(oxy)bis(5-oxopentanoic acid) (5)

Heptadecyl catechol (HDC, 2, 0.15 g) was dissolved in 10 mL of DCM, and glutaric anhydride (2.2 eq.) was added to the solution. Catalytic amounts of DMAP and triethylamine was then added and the reaction mixture was allowed to stir until TLC confirmed the complete conversion of the starting material to the product, 5, also referred to as HDC-hemiglutarate.

The reaction mixture was worked up as described above and the product was purified using column chromatography on silica gel and fractions containing the product were combined to give 180 mgs of the di-hemiglutarate ester of HDC (72%), (5).

The product was confirmed by HREIMS (TOF) m/z 575.3740 [M−H]⁺ (calculated for C₃₃H₅₂O₈, 575.3731) and by other spectral analysis techniques.

10 mg of dihemigluturate ester of HDC formed a homogenous solution when dissolved in 50 ul of ethanol and the resulting solution adjusted to 1 ml with potassium phosphate buffer (pH 8).

Example 7

Preparation of HDC-indole-propionate ester (6)

Heptadecyl catechol (HDC, 2, 0.20 g) was dissolved in 10 mL of DCM, and indole propionic acid (2.2 eq.) was added to the solution. Catalytic amount of DMAP, along with (2.2 eq.) of DCC was then added and the reaction mixture was allowed to stir until TLC confirmed the complete conversion of the starting material to the product.

The reaction mixture was worked up as usual and the product was purified using column chromatography on silica gel and fractions containing the product were combined to give of the product (90%). The product was confirmed by HREIMS (TOF) m/z 725.4248 [M+Cl]⁻ (calculated for C₄₅H₅₈Cl N₂O₄, 725.4080).

Example 8 Preparation of HDC-β-alaninate ester (7)

Heptadecyl catechol (HDC, 2, 0.10 g) was dissolved in 10 mL of DCM, and t-boc-β-alanine (2.2 eq.) was added to the solution. Catalytic amount of DMAP, along with (2.2 eq.) of DCC was then added and the reaction mixture was allowed to stir until TLC confirmed the complete conversion of the starting material to the product.

The reaction mixture was worked up as described and the product was purified using column chromatography on silica gel and fractions containing the product were combined to yeild the product (85%).

Deprotection of t-boc was accomplished as described earlier. The acetone crystallization procedure is repeated to get the pure product. The product was confirmed by HREIMS (TOF) m/z 490.3371 [M+H]⁺ (calculated for C₂₉H₅₁N₂O₄, 491.4072).

Example 9 Preparation of PDC-valininate ester (8)

Pentadecyl catechol (PDC, 1, 0.25 g) was dissolved in 20 mL of DCM, and t-boc-L-valine (2.2 eq) is added to the solution. Catalytic amount of DMAP, along with (2.2 eq) of DCC was then added and the reaction mixture was allowed to stir until TLC confirms the complete conversion of the starting material to the product.

The product was confirmed by HREIMS (TOF) m/z 719.5220 [M+H]⁺ (calculated for C₄₁H₇₁N₂O₈, 719.5205).

The t-Boc protected product was purified using column chromatography on silica gel and monitoring the fractions by TLC.

Deprotection of t-boc was accomplished as described previously. The acetone crystallization procedure was repeated to get the pure product. The product was confirmed by HREIMS (TOF) m/z 519.4224 [M+H]⁺ (calculated for C₃₁H₅₅N₂O₅, 519.4956).

Example 10 Preparation of PDC-di-valininate ester (9)

PDC-valine was dissolved in 20 mL of DCM, and t-boc-L-valine (2.2 eq) was added to the solution. Catalytic amount of DMAP, along with (2.2 eq) of DCC was then be added and the reaction mixture was allowed to stir until TLC confirms the complete conversion of the starting material to the product.

The t-Boc protected product was purified using column chromatography on silica gel and monitoring the fractions by TLC. The product was confirmed by HREIMS (TOF) m/z 917.6553 [M+H]⁺ (calculated for C₅₉H₈₉N₄O₁₀, 917.6573).

Deprotection of t-boc was accomplished by the procedure described earlier. The acetone crystallization procedure was repeated to get the pure product. The product was confirmed by HREIMS (TOF) m/z 717.5561 [M+H]⁺ (calculated for C₄₁H₇₃N₄O₆, 717.5525).

Example 11 Preparation of PDC-glutaminate ester (10)

Pentadecyl catechol (PDC, 1, 0.05 g) was dissolved in 10 mL of DCM, and t-boc-L-glutamine (2.2 eq) was added to the solution. Catalytic amount of DMAP, along with (2.2 eq) of DCC was then added and the reaction mixture was allowed to stir until TLC confirmed the complete conversion of the starting material to the product.

The t-boc protected product was purified using column chromatography on silica gel and monitoring the fractions by TLC.

Deprotection of t-boc was accomplished by the procedure described earlier. The acetone crystallization procedure was repeated to get the pure product. The product formed was confirmed by HREIMS (TOF) m/z 577.3966 [M−H]⁺ (Calculated for C₃₁H₅₃N₄O₆, 577.3960).

Example 12 Preparation of PDC-asparaginate ester (11)

Pentadecyl catechol (PDC, 1, 0.05 g) was dissolved in 10 mL of DCM, and t-boc-L-asparagine (2.2 eq) was added to the solution. Catalytic amount of DMAP, along with (2.2 eq) of DCC was then added and the reaction mixture was allowed to stir until TLC confirmed the complete conversion of the starting material to the product.

The t-Boc protected product was purified using column chromatography on silica gel and monitoring the fractions by TLC.

Deprotection of t-boc was accomplished as described previously. The acetone crystallization procedure was repeated to get the pure product. The product formed was confirmed using LC/MS m/z 549.5 [M+H]⁺.

Example 13 Preparation of PDC-glutaminate-β-alanine dipeptide ester (12)

PDC-glutaminate ester (10) was dissolved in 8 mL of DCM, and t-boc-β-alanine (2.2 eq) was added to the solution. Catalytic amount of DMAP, along with (2.2 eq) of DCC was then added and the reaction mixture was allowed to stir until TLC confirmed the complete conversion of the starting material to the product.

The t-boc protected product was purified using column chromatography on silica gel and monitoring the fractions by TLC.

Deprotection of t-boc was accomplished as described previously. The acetone crystallization procedure was repeated to get the pure product. The product formed was confirmed using LC/MS m/z 719.6 [M+H]⁺.

Example 14 Induction of tolerance to poison ivy/poison oak urushiol using water soluble derivatives of 3-n-heptadecylcatechol in the guinea pig contact dermatitis model

Specifically, three derivatives of 3-n-heptadecylcatechol (HDC, the saturated congener of poison oak urushiol) have been prepared and tested, namely: HDC phenyl alaninate ester (3), HDC hemiglutarate ester (5) and HDC 4-(4-aminophenyl)butyrate ester (4). A guinea pig animal model has been used to evaluate these agents activity vis-à-vis contact dermatitis and other biological activity.

Animals: Hartley strains of guinea pigs (n=40) were obtained from Harlan, Indianapolis Ind. 46229. The animals were divided in the 5 groups (n=8/group) and treated as described hereunder. These animals were kept in a controlled environment with a 12-hour day and night cycle and provided feed and water ad libitum. Study design: Diagram 1 describes the general procedure for determining the efficacy of the agents produced according to the present invention. As can be seen, HDC derivatives are injected at week 0, followed by a sensitization at 2 weeks, and subsequent urushiol challenges in subsequent weeks.

Group I. Animals in this group were given the compound (4) (HDC 4-(4-aminophenyl) butyrate ester) via the intramuscular (IM) route; 300μl of the equivalent of 20 mg/mL solution of the free catechol in 5% ethanol in each hind leg. Two weeks later these animals were sensitized with urushiol (100 μL acetone containing 1.0 mg of urushiol) on the surface skin in the neck region. Two weeks later the animals were challenged with urushiol (15 μL volume acetone containing 3.0 μg, 4.5 μg or 6.0 μg) on the abdominal skin in a volume of 15 μL. The vehicle contained 15 μL of acetone (see diagram 2). The animals were tested 3 times after sensitization: Test #1 at two weeks post sensitization, test #2 conducted at four weeks post sensitization and test #3 was conducted twelve weeks post sensitization.

Group II. Animals were given 300 μL of the equivalent of 20 mg/mL solution of the free catechol in 5% ethanol of HDC Phenyl alaninate ester (compound 3) via the IM route in each hind leg (total 600 μL). This was followed by sensitization with urushiol on the neck, and then tested with urushiol challenge on the abdominal skin as described for group I.

Group III. Animals were given 300 μL of the equivalent of 20 mg/mL solution of the free catechol in 5% ethanol of HDC Hemiglutarate ester (compound 5) via the IM route in each hind leg. This was followed, two weeks later, by sensitization with (urushiol 100 μL) on the neck, followed by abdominal skin test as described for group I.

Group IV. Animals were given 300 μL of vehicle (5% ethanol) via the IM route in each of the hind legs. This was followed, two weeks later, by sensitization and then followed by abdominal skin test as described for group I.

Group V. Animals in this group were given PBS (300 μL in each of the hind legs) via the IM route. This was followed two weeks later by sensitization and then followed by abdominal skin test as described for group I.

After challenging the animals with urushiol on their abdominal skin, the severity of Erythema and Edema were observed and scored according to the Draize scoring system as shown below. The scores were recorded at 24, 48 and 72 hrs post urushiol skin application.

Skin Lesion Observed Score No Erythema 0 Very Slight (Barely perceptible) Erythema 1 Well defined Erythema 2 Moderate to severe Erythema 3 Severe Erythema (beet red) Eschar 4 formation (deep injury) No Edema 0 Very slight edema (barely perceptible) 1 Well defined (edges of area will defined 2 by definite raising) Moderate edema (area raised approximately 3 l mm) Severe Edema (raised more than l mm and 4 extending beyond area of exposure) Maximum summed Erythema and Edema Scores = 8

RESULTS: The results are given in Tables 1A, B, C (for scores at 24, 48 and 72 hour post challenge respectively) through Tables 3A, B, C and FIGS. 1A, B, C through 3A, B, C. (Pictures taken at 72 hours post urushiol challenge from test #3 are also shown in FIG. 4A-E for illustration of the severity of reaction in the untreated groups IV and V relative to the treated groups I, II and III).

Test #1: The three treated groups of guinea pigs Groups I, II and III when challenged with different doses (3.0 μg, 4.5 μg and 6.0 μg) of urushiol on the abdominal skin did not show any or showed very slight erythema at the exposure site either at 24, 48 or 72 hrs post challenge. In contrast, animals of group IV and V showed varying degrees of erythema and edema. At 24 hours, the skin lesion score in group IV was lower than that of group V at challenge doses of 3.0 and 4.5 μg urushiol. However, there was no difference in the scores of these two groups at the challenge dose of 6.0 μg. As expected the vehicle (acetone) showed no reaction. At 48 hours post challenge, no erythema or edema was observed in the three prophylactic treated groups I, II and III. The skin lesion scores of these groups remained below 1.0. In groups IV and V the lesion scores were higher with the increasing concentration of urushiol challenge. In groups IV and V the skin lesion scores were comparable but tended to be slightly higher in group V. At 72 hours post challenge, no erythema or edema was observed in groups I, II and III. The skin lesion score remained below 1.0. In groups IV and V the skin lesion score were comparable but tended to be slightly higher in group V.

Comparison of lesion scores of groups IV and V at different time points indicates that maximum erythema and edema was observed at 48 hours. At 72 hrs the lesions tended to subside compared to that at 48 hours.

Test #2: This test was conducted two weeks after test #1. At 24 hours, the skin lesion score of group I, II and III (prophylactically treated) was below 1.0. In group IV (vehicle) the scores were 2.5, 3.0 and 3.5 when exposed to urushiol doses of 3.0, 4.5 and 6.0 μg, respectively. In group V the scores were 1.0, 4.0 and 6.5 with urushiol doses of 3.0, 4.5 and 6.0 μg, respectively. At 48 hours, group I showed a total score of 1.5 at the challenge doses of 4.5 or 6.0 μg urushiol. The skin lesion score of animals in group II did not exceed 1.0. In group III the total score was 1.0 and 2.5 with urushiol doses of 4.5 and 6.0 μg, respectively. These scores were comparatively lower than those of groups IV and V. In group V the total scores were 1.0, 4.0 and 6.5 in response to urushiol doses of 3.0, 4.5 and 6.0 μg, respectively.

At 72 hours, the lesions tended to regress. The total lesion score in groups I and II did not exceed 1.0 and in group III regressed to a maximum of 2.0. In groups IV and V the skin lesion scores regressed and ranged between 0.5 and 2.0. Comparatively, these scores were relatively higher than in the prophylactically treated groups I, II and III.

Test #3: This test was conducted approximately seven weeks after the last test #2. At 24 hours group I, II and III did not show erythema or edema at the site of urushiol challenge at any of the doses used. Animals in groups IV showed lesion scores of 2.0, 5.0 and 9.0 to the respectively increasing doses used in this study. The scores of skin lesions in group V were comparable to that in group IV, 2.5, 4.0 and 7.0 to the respective doses of urushiol used.

At 48 hours, the lesion score in group I and III remained below 1.0 and in group II did not exceed 1.0. However, in groups IV and V the skin lesions were, relatively, more pronounced; in group IV the sum of lesion score was 11.5, 20.5 and 29.5 to the respective doses of urushiol used. Similarly, the lesion scores in group V summed up to 6.0, 16.0 and 23.5 to the three respective doses of urushiol challenge.

At 72 hours, the scores in groups I, II and III regressed to below 1.0 or did not exceed 1.0. In contrast, scores of group IV and V remained relatively elevated; in these groups the maximum response to urushiol challenge dose was 28.5 and 22.5 respectively.

The skin lesion scores in group I, II and III in all the 3 tests were negligible compared to those in groups IV and V. This indicates that intramuscular injection of any of the 3 test compounds protected the animals against poison ivy dermatitis. All three compounds were equally effective as no remarkable difference was observed in the skin lesion scores of these three groups.

The skin lesions of groups IV and V in test #1 and test #2 were not as severe compared to that in test #3. It is possible that the massive sensitizing dose of urushiol (1.0 mg) on the neck may have caused a state of “anergy”. This condition is observed in patients of tuberculosis (TB) who are burdened with huge amount of TB antigen, but show no reaction to intradermal TB test (False negative). In our experiments, sensitization of animals with massive dose of urushiol may have induced an anergic state for the first two testing periods. However, a rest period of 11 weeks between sensitization and test #3 perhaps reversed the anergic state to a normal reactive state. Thus in test #3, animals in groups IV and V exhibited relatively stronger skin reactions to urushiol challenge; however, animals in group I, II and III were protected due to the prophylactic treatment (see photos of the reactivity of the different groups to the 3^(rd) challenge, 72 hour post topical application of test doses).

Example 15 Desensitization to poison ivy/oak urushiol of already sensitive guinea pigs using water soluble derivatives of 3-n-heptadecylcatechol

The control animal groups IV and V from the tolerance study (untreated with the derivatives), with established sensitivity (see Tables 3 A-C and FIGS. 4D and E) were used in this study to determine if IM administration of one of the water-soluble derivatives prepared would desensitize already sensitive animals.

Animals of group IV were injected 600 μL (300 μL in each hind leg) of HDC-4-(4-aminophenyl)-butyrate ester, 4, solution containing the equivalent of 20 mg/mL of HDC. Animals in group V were given 600 μL of vehicle (5% ethanol) divided in two doses of 300 μL in each hind leg. After a rest period of approximately 2 weeks animals in both groups were challenged by topical application of 3 doses of urushiol (3.0 μg, 4.5 μg and 6.0 μg dissolved in 15 μL of Acetone). At 24, 48 and 72 hrs post topical challenge skin lesions were observed and graded as described earlier.

RESULTS: The results are given in FIGS. 5 through 7 and Tables 4A-C. At 24 hrs no skin lesions were observed in animals of group IV; hence the total group score was zero for all doses. In group V, no skin reaction was observed with 3.0 μg urushiol. Very slight erythema was observed with 4.5 μg urushiol, the total group score being 1.0. Similarly, with urushiol dose of 6.0 μg total group score remained low at 2.5.

At 48 hours post topical challenge (FIG. 5B and Table 4B), no erythema was observed with 3.0 μg urushiol in both groups IV and V. At 4.5 μg urushiol challenge, total score of group IV was 0.5 but of group V was 4.0. At 6.0 μg dose of urushiol the total score of group IV remained at 0.5, however, in group V, it elevated to 6.5.

At 72 hours post urushiol challenge, the total score of group IV remained between zero and 1.5 at all the doses of urushiol challenge. The total skin lesion score of animals in groups V was elevated to 18.5, especially at the 6.0 μg dose.

The skin reaction in response to urushiol challenge in group IV animals was negligible compared to that in Group V. This was especially obvious at 72 hours post urushiol challenge at the highest dose (6.0 μg) (FIGS. 6 and 7). These results indicate that IM injection of the test compound protected the animals in group IV against urushiol contact dermatitis reaction. In contrast, the control animals in group V exhibited a strong skin reaction. This indicates that IM injection of the test compound HDC 4-(4-aminophenyl)-butyrate ester, 4, effectively desensitized previously reactive animals.

Example 16 Stability of Compounds 3, 4, And 5

All derivatives prepared were subjected to a stability study to ascertain if one compound would have the advantage of long shelf life, especially at room temperature.

Aqueous solutions (in 5% EtOH) of the three compounds were prepared at a concentration of the equivalent of 10 mg/mL of HDC. For each compound 250 μL aliquots were transferred into glass vials and the material was freeze dried and the vials capped and stored at room temperature (20-24° C.).

Individual vials were then removed at certain time points, reconstituted with distilled water to dissolve the residue and the solutions subjected to HPLC analysis. The chromatographic conditions are such that it is easy to determine if degradation (hydrolysis) has taken place. The samples were analyzed at time 0, 1 month, 3 months and 6 months, 9 months, 12 months, 18 months, and 24 months.

RESULTS: The data showed that HDC phenylalaninate 2.HCl (3) and HDC-4-(4-aminophenyl)-butyrate 2.HCl (4) were very stable at room temperature (20-24° C.) in the freeze dried state with >99% of the original amount at time 0 present in the ester form after 24 months of room temperature storage. On the other hand HDC-hemiglutarate 2Na⁺, (5) was less stable under the same conditions. After one month 8.3% of the ester form was hydrolyzed and 29.3% and 44.4% of the time 0 material was hydrolyzed at 3 and 6 months respectively. Therefore, the amino acid derivatives are more stable and would afford longer shelf life.

Example 17 Preparation of Injectable Formulations Compatible With the Human Use

The formulations prepared for the animal studies were based on the use of the salts of the two compounds (HCl salts for the phenyl alaninate ester (3) and the 4-(4-aminophenyl)butyrate ester (4)). These salts dissolve easily in ethanol. The ethanolic solutions were mixed with distilled water to make the final solutions having alcohol concentrations being only 5%.

Although this formulation is acceptable for human use, we have prepared several other formulations in which the fmal solution is isotonic. These formulations include different other solubilizing (stabilizing) agents and are compared to the original 5% ethanolic solution used in animal studies. The following vehicles were used to prepare solutions of compounds (3) and (4) at 20 mg/ml.

 5% ethanol in water Made isotonic with NaCl  5% propylene glycol Made isotonic with NaCl 10% propylene glycol Made isotonic with NaCl  5% polyethylene glycol 400 Made isotonic with NaCl (PEG 400) 10% PEG 400 Made isotonic with NaCl

Both propylene glycol and PEG 400 have been used to prepare injectables and are considered by the FDA as safe (GRAS) for these applications.

All vehicles were able to dissolve both compounds where a 20 mg/ml solution was formed as clear solution at room temperature and therefore any of the above vehicles could be used to prepare injectable solutions of these compounds.

Representative delivery regimens for the present active agents include parenteral (including subcutaneous, intramuscular and intravenous), transdermal, and intranasal.

Pharmaceutically acceptable salts retain the desired biological activity of the active material without toxic side effects. Examples of such salts are (a) acid addition salts formed with inorganic acids, for example hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; and salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, pamoic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acids, naphthalene disulfonic acids, polygalacturonic acid and the like; (b) base addition salts formed with mono- and polyvalent metal cations such as sodium, potassium, zinc, calcium, magnesium, and the like.

A further aspect of the present invention relates to pharmaceutical compositions comprising an active ingredient of the present invention, as a pharmaceutically acceptable salt thereof, in admixture with a pharmaceutically acceptable, non-toxic carrier. Such compositions may be prepared for parenteral (subcutaneous, intramuscular or intravenous) administration, particularly in the form of liquid solutions as nasal drops or aerosols.

The compositions may conveniently be administered in unit dosage form and may be prepared by any of the methods well-known in the pharmaceutical art, for example as described in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., (1985). Formulations for parenteral administration may contain as excipients sterile water or saline, alkylene glycols such as propylene glycol, polyalkylene glycols such as polyethylene glycol, and the like. Formulations for nasal administration may be solid and may contain excipients, for example, lactose or dextran, or may be aqueous solutions for use in the form of nasal drops or metered spray.

When formulated for nasal administration, the absorption across the nasal mucous membrane may be enhanced by surfactant acids, such as for example, glycocholic acid, cholic acid, taurocholic acid, ethocholic acid, deoxycholic acid, chenodeoxycholic acid, dehydrocholic acid, glycodeoxycholic acid, cyclodextrins and the like.

Other material, such as preservatives, salts to achieve isotonicity, buffers, and the like, may be added to the parenteral and nasal formulations.

The actual dosage amount administered can be determined by physical and physiological factors such as body weight, severity of condition, and idiopathy of the patient. With these considerations in mind, the dosage of the actives of this invention for a particular subject and or course of treatment can readily be determined.

CONCLUSION

In the foregoing description, certain terms and visual depictions are used to illustrate the preferred embodiment. However, no unnecessary limitations are to be construed by the terms used or illustrations depicted, beyond what is shown in the prior art, since the terms and illustrations are exemplary only, and are not meant to limit the scope of the present invention. It is further known that other modifications may be made to the present invention, without departing the scope of the invention, as noted in the appended claims. All references and citations mentioned in this application are hereby incorporated in total herein.

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1. Compounds effective for desensitizing a subject against contact dermatitis caused by allergens contained in plants of the Anacardiaceae and Ginkgoaceae families comprising water-soluble urushiol esters of the following formula I

wherein R₁ is an alkyl radical having 11 to 19 carbon atoms, or an unsaturated congener thereof; or mixtures thereof; and R₂ and R₃ are each independently the residue radicals derived from an amino acid or a combination of amino acids, a carbamate-forming compound, an ester of a dicarboxylic acid or a dicarboxylic acid derivative or a sulfate or phosphate ester wherein the esters are salt forming compounds.
 2. Compounds of claim 1 wherein R₁ is pentadecyl.
 3. Compounds of claim 1 wherein R₁ is heptadecyl.
 4. Compounds of claim 1 wherein R₁ is nonadecyl.
 5. Compounds of claim 1, wherein the water-soluble esters are esters of amino acids or combinations of amino acids or derivatives of an amino acid with a dicarboxylic acid.
 6. Compounds of claim 1, wherein the water-soluble esters are esters of dicarboxylic acids or dicarboxylic acid derivatives.
 7. Compounds of claim 1, wherein the water-soluble esters are phosphate or sulfate esters.
 8. Compounds of claim 1, wherein the water-soluble esters are salt-forming carbamates.
 9. Compounds according to claim 1 wherein the compound is heptadecyl catechol phenyl alaninate ester, 3-hepta-1,2-phenylene bis (4-aminophenyl) butanoate, heptadecyl catechol indole-propionate ester, heptadecyl catechol-β-alaninate ester, pentadecyl catechol valininate ester, pentadecyl catechol-di-valininate ester, pentadecyl catechol glutaminate ester, pentadecyl catechol asparaginate ester, pentadecyl catechol glutaminate-β-alanine dipeptide ester.
 10. A pharmaceutical composition comprising at least one compound according to claim 1 and suitable pharmaceutical carrier therefor.
 11. The composition of claim 10 wherein the composition is adapted to be administered parenterally, transdermally or intranasally.
 12. A method of desensitizing a subject to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families which comprises administering to said subject a composition comprising a compound or mixture of compounds according to claim
 1. 13. The method of claim 12 wherein, the composition is administered parenterally, transdermally or transnasally.
 14. The method of desensitizing a subject to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families which comprises administering to said subject, a pharmaceutical composition according to claim
 10. 15. A method of preparing compounds according to claim 5 comprising reacting a compound of the formula II

wherein R₁ is as defined in claim 1, with a protected amino acid or a combination of protected amino acids or a derivative of a protected amino acid with a dicarboxylic acid or dicarboxylic acid derivative followed by removal of the protective group.
 16. A method of preparing compounds according to claim 6 comprising reacting a compound of the formula II

wherein R₁ is as defined in claim 1, with a dicarboxylic acid or dicarboxylic acid derivative.
 17. A method of preparing compounds according to claim 8 comprising reacting a compound of the formula II

wherein R₁ is as defined in claim 1, with para nitrophenyl chloroformate followed by reaction of this intermediate with an allyl ester of a amino acid or combination of amino acids followed by removal of the allyl group from the resulting product.
 18. A method of making the sulfate esters according to claim 7 comprising reacting a compound of the formula II

wherein R₁ is as defined in claim 1, with chlorosulfonic acid.
 19. The method of desensitizing a subject to allergens contained in plants of the Anacardiaceae and Ginkgoaceae families which comprises administering to said subject, a pharmaceutical composition according to claim
 11. 